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- Which of the following mechanisms is consistent with the reaction profile shown above? Circle the correct mechanism and justify your choice.Which is/are NOT TRUE about bimolecular nucleophilic substitution reactions? Select one or more: 1. A carbocation intermediate is formed. 2. A strong nucleophile displaces a halogen atom in a concerted mechanism. 3. Presence of polar aprotic solvents promotes this reaction. 4. Methyl halides react faster than secondary alkyl halides.What is product ? Please show mechanism each step
- Classify the type of elementary step based on the mechanistic arrow(s) shown below. A) homolytic B) heterolytic1 example for organic rearrangement reaction show: a. the overall reaction (reactants --> products) b. the reaction mechanism (indicate intermediate product) c. indicate which is the reactive species or intermediate in the reaction (radical? electrophile? nucleophile?) d. overall description of the reaction eg., radical substitution or SRWhich rxn would be fastest? Which would be slowest?
- Classify the type of elementary step based on the mechanistic arrow(s) shown below.i need this reaction mechanism draw plsShown below is a carbocation intermediate in an electrophilic addition reaction of HCl with an alkene. For the conformation shown, select each hydrogen whose bond to carbon is aligned for effective hyperconjugation with the vacant p orbital on the positively charged carbon. Each adjacent carbon will have only one C-H bond so aligned. I need to click on the Hydrogens which then highlights the clicked hydrogens in blue. Much help needed. There are hydrogens and carbons shown.